"Behcet Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well.
| Descriptor ID |
D001528
|
| MeSH Number(s) |
C07.465.075 C11.941.879.780.880.200 C14.907.940.100 C16.320.382.250 C17.800.827.368.250 C17.800.862.150
|
| Concept/Terms |
Behcet Syndrome- Behcet Syndrome
- Triple-Symptom Complex
- Behcet Disease
- Triple Symptom Complex
- Complex, Triple Symptom
- Complices, Triple Symptom
- Symptom Complex, Triple
- Symptom Complices, Triple
- Triple Symptom Complices
- Adamantiades-Behcet Disease
- Adamantiades Behcet Disease
- Adamantiades-Behcet Diseases
- Disease, Adamantiades-Behcet
- Diseases, Adamantiades-Behcet
- Behcet Triple Symptom Complex
- Old Silk Route Disease
- Behcet's Syndrome
- Behcets Syndrome
- Behçet Disease
- Behçet Diseases
- Disease, Behçet
- Diseases, Behçet
|
Below are MeSH descriptors whose meaning is more general than "Behcet Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Behcet Syndrome".
This graph shows the total number of publications written about "Behcet Syndrome" by people in this website by year, and whether "Behcet Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 2 | 0 | 2 |
| 2012 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Behcet Syndrome" by people in Profiles.
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Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease. Arthritis Rheumatol. 2021 07; 73(7):1244-1252.
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Juvenile spondyloarthropathies. Curr Rheumatol Rep. 2012 Oct; 14(5):395-401.
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A putative functional variant within the UBAC2 gene is associated with increased risk of Behçet's disease. Arthritis Rheum. 2011 Nov; 63(11):3607-12.
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IL18 polymorphism is associated with Behçet's disease but not lupus in patients from Turkey. J Rheumatol. 2011 May; 38(5):962-3.
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Acral purpuric papulonodular lesions as a manifestation of Behçet's disease. Int J Dermatol. 1995 Mar; 34(3):190-2.
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Cutaneous manifestations of Behçet's disease. Int J Dermatol. 1995 Mar; 34(3):159-65.